Utility of microsatellite analysis in evaluation of pregnancies with placental mesenchymal dysplasia

Prenatal Diagnosis

Volumn 27, Issue 13, 2007, Pages 1238-1244

  Schuetzle, Marie N ^a   Uphoff, Timothy S ^b   Hatten, Bonnie A ^c   Dawson, D Brian ^a  

^a MAYO CLINIC   (United States)

^b MARSHFIELD CLINIC   (United States)

^c ABBOTT NORTHWESTERN HOSPITAL   (United States)

Author keywords

Beckwith Wiedemann syndrome; Molecular microsatellite analysis; Placental mesenchymal dysplasia

Indexed keywords

ADULT; AMNION CELL; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CYTOGENETICS; DIAGNOSTIC PROCEDURE; DNA METHYLATION; DYSPLASIA; FEMALE; FETUS ECHOGRAPHY; FETUS KARYOTYPING; GENE AMPLIFICATION; GENETIC ANALYSIS; HUMAN; KARYOTYPE 46,XX; MICROSATELLITE MARKER; MOLECULAR GENETICS; MOLECULAR PROBE; PLACENTA DISORDER; PLACENTA MESENCHYME DYSPLASIA; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABORTION, THERAPEUTIC; ADULT; BECKWITH-WIEDEMANN SYNDROME; FEMALE; HUMANS; MICROSATELLITE REPEATS; PLACENTA DISEASES; PREGNANCY; PRENATAL DIAGNOSIS; ULTRASONOGRAPHY, PRENATAL; UNIPARENTAL DISOMY;

EID: 37349098286     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1879     Document Type: Article

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